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2024-04-19 01:54:19, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_017410 2435 bp mRNA linear PRI 07-JUL-2013 DEFINITION Homo sapiens homeobox C13 (HOXC13), mRNA. ACCESSION NM_017410 VERSION NM_017410.2 GI:24497535 KEYWORDS RefSeq. SOURCE Homo sapiens (human) ORGANISM Homo sapiens Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo. REFERENCE 1 (bases 1 to 2435) AUTHORS Lin,Z., Chen,Q., Shi,L., Lee,M., Giehl,K.A., Tang,Z., Wang,H., Zhang,J., Yin,J., Wu,L., Xiao,R., Liu,X., Dai,L., Zhu,X., Li,R., Betz,R.C., Zhang,X. and Yang,Y. TITLE Loss-of-function mutations in HOXC13 cause pure hair and nail ectodermal dysplasia JOURNAL Am. J. Hum. Genet. 91 (5), 906-911 (2012) PUBMED 23063621 REMARK GeneRIF: loss-of-function mutations in HOXC13 cause autosomal-recessive PHNED and further highlight the importance of HOXC13 in hair and nail development. REFERENCE 2 (bases 1 to 2435) AUTHORS Cantile,M., Scognamiglio,G., Anniciello,A., Farina,M., Gentilcore,G., Santonastaso,C., Fulciniti,F., Cillo,C., Franco,R., Ascierto,P.A. and Botti,G. TITLE Increased HOX C13 expression in metastatic melanoma progression JOURNAL J Transl Med 10, 91 (2012) PUBMED 22583695 REMARK GeneRIF: results show the strong and progressive HOX C13 overexpression in metastatic melanoma tissues and cytological samples compared to nevi and primary melanoma tissues and cells. Publication Status: Online-Only REFERENCE 3 (bases 1 to 2435) AUTHORS Chen,F., Li,Y., Wang,L. and Hu,L. TITLE Knockdown of BMI-1 causes cell-cycle arrest and derepresses p16INK4a, HOXA9 and HOXC13 mRNA expression in HeLa cells JOURNAL Med. Oncol. 28 (4), 1201-1209 (2011) PUBMED 20661663 REMARK GeneRIF: knockdown of BMI-1 expression can induce cell-cycle arrest and up-regulate p16INK4a, HOXA9 and HOXC13 in HeLa cells REFERENCE 4 (bases 1 to 2435) AUTHORS Heid IM, Jackson AU, Randall JC, Winkler TW, Qi L, Steinthorsdottir V, Thorleifsson G, Zillikens MC, Speliotes EK, Magi R, Workalemahu T, White CC, Bouatia-Naji N, Harris TB, Berndt SI, Ingelsson E, Willer CJ, Weedon MN, Luan J, Vedantam S, Esko T, Kilpelainen TO, Kutalik Z, Li S, Monda KL, Dixon AL, Holmes CC, Kaplan LM, Liang L, Min JL, Moffatt MF, Molony C, Nicholson G, Schadt EE, Zondervan KT, Feitosa MF, Ferreira T, Lango Allen H, Weyant RJ, Wheeler E, Wood AR, Estrada K, Goddard ME, Lettre G, Mangino M, Nyholt DR, Purcell S, Smith AV, Visscher PM, Yang J, McCarroll SA, Nemesh J, Voight BF, Absher D, Amin N, Aspelund T, Coin L, Glazer NL, Hayward C, Heard-Costa NL, Hottenga JJ, Johansson A, Johnson T, Kaakinen M, Kapur K, Ketkar S, Knowles JW, Kraft P, Kraja AT, Lamina C, Leitzmann MF, McKnight B, Morris AP, Ong KK, Perry JR, Peters MJ, Polasek O, Prokopenko I, Rayner NW, Ripatti S, Rivadeneira F, Robertson NR, Sanna S, Sovio U, Surakka I, Teumer A, van Wingerden S, Vitart V, Zhao JH, Cavalcanti-Proenca C, Chines PS, Fisher E, Kulzer JR, Lecoeur C, Narisu N, Sandholt C, Scott LJ, Silander K, Stark K, Tammesoo ML, Teslovich TM, Timpson NJ, Watanabe RM, Welch R, Chasman DI, Cooper MN, Jansson JO, Kettunen J, Lawrence RW, Pellikka N, Perola M, Vandenput L, Alavere H, Almgren P, Atwood LD, Bennett AJ, Biffar R, Bonnycastle LL, Bornstein SR, Buchanan TA, Campbell H, Day IN, Dei M, Dorr M, Elliott P, Erdos MR, Eriksson JG, Freimer NB, Fu M, Gaget S, Geus EJ, Gjesing AP, Grallert H, Grassler J, Groves CJ, Guiducci C, Hartikainen AL, Hassanali N, Havulinna AS, Herzig KH, Hicks AA, Hui J, Igl W, Jousilahti P, Jula A, Kajantie E, Kinnunen L, Kolcic I, Koskinen S, Kovacs P, Kroemer HK, Krzelj V, Kuusisto J, Kvaloy K, Laitinen J, Lantieri O, Lathrop GM, Lokki ML, Luben RN, Ludwig B, McArdle WL, McCarthy A, Morken MA, Nelis M, Neville MJ, Pare G, Parker AN, Peden JF, Pichler I, Pietilainen KH, Platou CG, Pouta A, Ridderstrale M, Samani NJ, Saramies J, Sinisalo J, Smit JH, Strawbridge RJ, Stringham HM, Swift AJ, Teder-Laving M, Thomson B, Usala G, van Meurs JB, van Ommen GJ, Vatin V, Volpato CB, Wallaschofski H, Walters GB, Widen E, Wild SH, Willemsen G, Witte DR, Zgaga L, Zitting P, Beilby JP, James AL, Kahonen M, Lehtimaki T, Nieminen MS, Ohlsson C, Palmer LJ, Raitakari O, Ridker PM, Stumvoll M, Tonjes A, Viikari J, Balkau B, Ben-Shlomo Y, Bergman RN, Boeing H, Smith GD, Ebrahim S, Froguel P, Hansen T, Hengstenberg C, Hveem K, Isomaa B, Jorgensen T, Karpe F, Khaw KT, Laakso M, Lawlor DA, Marre M, Meitinger T, Metspalu A, Midthjell K, Pedersen O, Salomaa V, Schwarz PE, Tuomi T, Tuomilehto J, Valle TT, Wareham NJ, Arnold AM, Beckmann JS, Bergmann S, Boerwinkle E, Boomsma DI, Caulfield MJ, Collins FS, Eiriksdottir G, Gudnason V, Gyllensten U, Hamsten A, Hattersley AT, Hofman A, Hu FB, Illig T, Iribarren C, Jarvelin MR, Kao WH, Kaprio J, Launer LJ, Munroe PB, Oostra B, Penninx BW, Pramstaller PP, Psaty BM, Quertermous T, Rissanen A, Rudan I, Shuldiner AR, Soranzo N, Spector TD, Syvanen AC, Uda M, Uitterlinden A, Volzke H, Vollenweider P, Wilson JF, Witteman JC, Wright AF, Abecasis GR, Boehnke M, Borecki IB, Deloukas P, Frayling TM, Groop LC, Haritunians T, Hunter DJ, Kaplan RC, North KE, O'Connell JR, Peltonen L, Schlessinger D, Strachan DP, Hirschhorn JN, Assimes TL, Wichmann HE, Thorsteinsdottir U, van Duijn CM, Stefansson K, Cupples LA, Loos RJ, Barroso I, McCarthy MI, Fox CS, Mohlke KL and Lindgren CM. CONSRTM MAGIC TITLE Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution JOURNAL Nat. Genet. 42 (11), 949-960 (2010) PUBMED 20935629 REMARK GeneRIF: Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) Erratum:[Nat Genet. 2011 Nov;43(11):1164] REFERENCE 5 (bases 1 to 2435) AUTHORS Garcia-Barcelo,M.M., Yeung,M.Y., Miao,X.P., Tang,C.S., Cheng,G., So,M.T., Ngan,E.S., Lui,V.C., Chen,Y., Liu,X.L., Hui,K.J., Li,L., Guo,W.H., Sun,X.B., Tou,J.F., Chan,K.W., Wu,X.Z., Song,Y.Q., Chan,D., Cheung,K., Chung,P.H., Wong,K.K., Sham,P.C., Cherny,S.S. and Tam,P.K. TITLE Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2 JOURNAL Hum. Mol. Genet. 19 (14), 2917-2925 (2010) PUBMED 20460270 REMARK Erratum:[Hum Mol Genet. 2011 Mar 1;20(5):1048. Chen, Guo [corrected to Cheng, Guo]] REFERENCE 6 (bases 1 to 2435) AUTHORS de Stanchina,E., Gabellini,D., Norio,P., Giacca,M., Peverali,F.A., Riva,S., Falaschi,A. and Biamonti,G. TITLE Selection of homeotic proteins for binding to a human DNA replication origin JOURNAL J. Mol. Biol. 299 (3), 667-680 (2000) PUBMED 10835276 REFERENCE 7 (bases 1 to 2435) AUTHORS Godwin,A.R. and Capecchi,M.R. TITLE Hair defects in Hoxc13 mutant mice JOURNAL J. Investig. Dermatol. Symp. Proc. 4 (3), 244-247 (1999) PUBMED 10674376 REMARK Review article REFERENCE 8 (bases 1 to 2435) AUTHORS Apiou,F., Flagiello,D., Cillo,C., Malfoy,B., Poupon,M.F. and Dutrillaux,B. TITLE Fine mapping of human HOX gene clusters JOURNAL Cytogenet. Cell Genet. 73 (1-2), 114-115 (1996) PUBMED 8646877 REFERENCE 9 (bases 1 to 2435) AUTHORS Acampora,D., D'Esposito,M., Faiella,A., Pannese,M., Migliaccio,E., Morelli,F., Stornaiuolo,A., Nigro,V., Simeone,A. and Boncinelli,E. TITLE The human HOX gene family JOURNAL Nucleic Acids Res. 17 (24), 10385-10402 (1989) PUBMED 2574852 REFERENCE 10 (bases 1 to 2435) AUTHORS Rabin,M., Ferguson-Smith,A., Hart,C.P. and Ruddle,F.H. TITLE Cognate homeo-box loci mapped on homologous human and mouse chromosomes JOURNAL Proc. Natl. Acad. Sci. U.S.A. 83 (23), 9104-9108 (1986) PUBMED 2878432 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AF255676.1, AF263466.2, BU158600.1, BC090850.1 and AA722686.1. This sequence is a reference standard in the RefSeqGene project. On Nov 3, 2002 this sequence version replaced gi:8393553. Summary: This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, which are located on different chromosomes and consist of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXC genes located in a cluster on chromosome 12. The product of this gene may play a role in the development of hair, nail, and filiform papilla. [provided by RefSeq, Jul 2008]. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: AF255676.1, AK024027.1 [ECO:0000332] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-399 AF255676.1 1-399 400-1119 AF263466.2 357-1076 1120-1468 BU158600.1 409-757 1469-2144 BC090850.1 1438-2113 2145-2155 AA722686.1 244-254 c 2156-2435 AF263466.2 2112-2391 FEATURES Location/Qualifiers source 1..2435 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="12" /map="12q13.3" gene 1..2435 /gene="HOXC13" /gene_synonym="ECTD9; HOX3; HOX3G" /note="homeobox C13" /db_xref="GeneID:3229" /db_xref="HGNC:5125" /db_xref="MIM:142976" exon 1..851 /gene="HOXC13" /gene_synonym="ECTD9; HOX3; HOX3G" /inference="alignment:Splign:1.39.8" STS 42..1335 /gene="HOXC13" /gene_synonym="ECTD9; HOX3; HOX3G" /db_xref="UniSTS:490461" variation 78 /gene="HOXC13" /gene_synonym="ECTD9; HOX3; HOX3G" /replace="c" /replace="g" /db_xref="dbSNP:200404690" misc_feature 92..94 /gene="HOXC13" /gene_synonym="ECTD9; HOX3; HOX3G" /note="upstream in-frame stop codon" CDS 116..1108 /gene="HOXC13" /gene_synonym="ECTD9; HOX3; HOX3G" /note="homeo box 3G; NUP98/HOXC13; homeobox protein Hox-3G" /codon_start=1 /product="homeobox protein Hox-C13" /protein_id="NP_059106.2" /db_xref="GI:24497536" /db_xref="CCDS:CCDS8865.1" /db_xref="GeneID:3229" /db_xref="HGNC:5125" /db_xref="MIM:142976" /translation="
MTTSLLLHPRWPESLMYVYEDSAAESGIGGGGGGGGGGTGGAGGGCSGASPGKAPSMDGLGSSCPASHCRDLLPHPVLGRPPAPLGAPQGAVYTDIPAPEAARQCAPPPAPPTSSSATLGYGYPFGGSYYGCRLSHNVNLQQKPCAYHPGDKYPEPSGALPGDDLSSRAKEFAFYPSFASSYQAMPGYLDVSVVPGISGHPEPRHDALIPVEGYQHWALSNGWDSQVYCSKEQSQSAHLWKSPFPDVVPLQPEVSSYRRGRKKRVPYTKVQLKELEKEYAASKFITKEKRRRISATTNLSERQVTIWFQNRRVKEKKVVSKSKAPHLHST
"
misc_feature 896..1051
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/note="Homeodomain; DNA binding domains involved in the
transcriptional regulation of key eukaryotic developmental
processes; may bind to DNA as monomers or as homo- and/or
heterodimers, in a sequence-specific manner; Region:
homeodomain; cd00086"
/db_xref="CDD:28970"
misc_feature order(896..910,914..916,965..967,983..985,1022..1024,
1028..1033,1040..1045,1049..1051)
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/note="DNA binding site [nucleotide binding]"
/db_xref="CDD:28970"
misc_feature order(902..904,911..913,1031..1033,1040..1045)
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/note="specific DNA base contacts [nucleotide binding];
other site"
/db_xref="CDD:28970"
variation 162..163
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace=""
/replace="tat"
/db_xref="dbSNP:34421542"
variation 169
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="c"
/replace="g"
/db_xref="dbSNP:375128529"
variation 176
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="g"
/db_xref="dbSNP:202210130"
variation 198..199
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace=""
/replace="cgg"
/db_xref="dbSNP:34115456"
variation 264
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1867298"
variation 354
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="g"
/db_xref="dbSNP:369377519"
variation 396
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="c"
/db_xref="dbSNP:35956662"
STS 464..543
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/standard_name="Hoxc13"
/db_xref="UniSTS:536660"
variation 484
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="c"
/db_xref="dbSNP:201389826"
variation 523
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="c"
/replace="t"
/db_xref="dbSNP:372818306"
variation 560
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="c"
/replace="t"
/db_xref="dbSNP:371276587"
variation 642
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="c"
/db_xref="dbSNP:373214679"
variation 664
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="c"
/replace="g"
/db_xref="dbSNP:199766120"
variation 707
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="g"
/db_xref="dbSNP:374868388"
variation 824
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="c"
/replace="g"
/db_xref="dbSNP:199770484"
exon 852..2396
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/inference="alignment:Splign:1.39.8"
variation 887
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="c"
/replace="t"
/db_xref="dbSNP:376143725"
variation 892
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="c"
/replace="t"
/db_xref="dbSNP:369582535"
variation 917
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="c"
/db_xref="dbSNP:376367135"
variation 955
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:140009861"
variation 1086
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="c"
/replace="t"
/db_xref="dbSNP:201149022"
variation 1092
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="g"
/db_xref="dbSNP:200110160"
variation 1119
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="g"
/db_xref="dbSNP:202061690"
variation 1120
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="c"
/db_xref="dbSNP:4759058"
variation 1132
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="t"
/db_xref="dbSNP:375338990"
variation 1172
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="g"
/db_xref="dbSNP:17105382"
variation 1195
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="g"
/db_xref="dbSNP:113894846"
variation 1305
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="c"
/db_xref="dbSNP:148556113"
variation 1461
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="g"
/replace="t"
/db_xref="dbSNP:182201998"
variation 1548
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="c"
/replace="t"
/db_xref="dbSNP:377375228"
variation 1576
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="c"
/replace="t"
/db_xref="dbSNP:186940213"
variation 1621
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace=""
/replace="tttctgtgcgtattttaaaagtcgtg"
/db_xref="dbSNP:11275538"
variation 1682
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2241937"
STS 1845..2148
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/standard_name="RH122467"
/db_xref="UniSTS:135339"
variation 1897
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="c"
/replace="t"
/db_xref="dbSNP:192503371"
variation 1898..1899
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace=""
/replace="ct"
/db_xref="dbSNP:146279895"
variation 2055
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="c"
/replace="g"
/db_xref="dbSNP:114528288"
variation 2073
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="c"
/replace="t"
/db_xref="dbSNP:373827912"
variation 2125
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="t"
/db_xref="dbSNP:142996820"
variation 2145
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1822437"
STS 2153..2350
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/standard_name="STS-AA024448"
/db_xref="UniSTS:83330"
variation 2153
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="c"
/replace="t"
/db_xref="dbSNP:11942"
variation 2278
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="t"
/db_xref="dbSNP:183862639"
variation 2356
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1054251"
polyA_signal 2372..2377
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
variation 2382
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace="a"
/replace="c"
/db_xref="dbSNP:370027588"
variation 2390..2391
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/replace=""
/replace="g"
/db_xref="dbSNP:5798291"
polyA_site 2396
/gene="HOXC13"
/gene_synonym="ECTD9; HOX3; HOX3G"
/experiment="experimental evidence, no additional details
recorded"
ORIGIN
aggggtggagagaaaagaggggagggatggggggaggggaaacaggagcgaggtgtctccctagctcgctgcctctggcaagtggagtttttaaaaagctccagcagatcatgtcatgacgacttcgctgctcctgcatccacgctggccggagagccttatgtacgtctatgaggacagcgcggcggagagcggcatcggcggcggcggcggaggaggaggcggcggcacgggcggagcggggggtggctgcagcggagcgagccccggcaaagccccgagcatggatggtctgggcagcagctgcccggccagccactgccgcgacctgcttccgcaccccgtgctgggccgcccgccggctcccctgggcgcccctcagggcgccgtctatacggacatcccggccccggaggcggcgcgccagtgtgccccgccgcccgcaccccccacctcgtccagcgccaccctgggctacggctaccccttcgggggcagctactacggctgccgcctgtcgcacaacgtgaacctgcagcagaagccttgcgcctaccacccgggcgataaatacccggagccgtcgggcgccctgcccggtgacgacctgtcctctagggccaaggagttcgccttctaccccagcttcgccagctcctaccaggcgatgcccggctacctggacgtgtcggtggtgcccgggatcagcgggcacccggagccgcgtcacgacgccctcatccccgtcgaaggctaccagcactgggctctctccaatggctgggacagtcaggtgtactgctccaaggagcagtcgcagtccgcccacctctggaagtctcccttcccagacgtggttcccctgcagcccgaggtgagcagctaccggcgcgggcgcaagaaacgcgtgccctacactaaggtgcagctgaaggagctagagaaggaatacgcggctagcaagttcatcaccaaagagaagcgccggcgcatctccgccaccacgaacctctctgagcgccaggtaaccatctggttccagaaccggcgggtcaaagagaagaaggtggtcagcaaatcgaaagcgcctcatctccactccacctgaccacccacccgctgcttgccccatctatttatgtctccgctttgtaccataaccgaacccacggaaagacgctgcgcgggtgcagaagagtatttaatgttaaggaaagagaagaaccgcgccgcccggaggcagagaggctccatggccgtgctgctgggccatccccaactccctatcccatccccagcctccacccccatccagatgggactcacgtggcttcaacagctttggaaatgggtcccgagtgggccgtgcgaggaaggctgtcgacctctactcctccttgcgctcaccttgccagaaagtctggtggcagcgcagagcccaatcattccaaccaaagcagggttggggaatcccgaatggccccaattcttgcctcatcctatgaccaggcttttagaggaccttccctaagggcgcagcttcggagcaggatctgtccagctcatactttccttcgctgtccctcccgcactccttaggcaagatttcccagtaaagattttctgtgcgtattttaaaagtcgtgttaatactcatgataattattagggacctggcagcgtgattggagtatggatgtttccgtaaaagctggaattccgtaaaagcattgacgcagcccctacactccatcccaaccaagaaactgcatttcctggggccaggtgggagctgcctttgccccactgcctcccctgttctgctctctcagtcaacatgtggaaatccaaggaggacaaagactccagccacgctgctaaatagggctcctctctcctctctctctctctaggtggtaaggttggggattagtccaggtacagaagcagaacttttttctaaggataaacatctcttccaaggggatggagagtgggtccctcaacaaagtccctgtccagtcacctttccatcagggcactagcccaggaatgactcctcacactttcacctttactgatttccagaggaaagctagaggatctagttcaagaggcaagaagatctggccctcaattagctagatgtagatgctgcctaacagttccctcctcaaaggccaccttggtgctgtgggggccccttgcctcttcccttcccactggtgcattacaaaacagtgttcttttgaaatgttcatcaggaataggcttttttaaaaaatgttgtgtatctgtatatagtattgtgatgtctgaatgacaatgtactgaatgcaaaaaggaaaaaaacccacaaacatgtttttaaaataaaatatctttttttgccttgaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:3229 -> Molecular function: GO:0001077 [RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in positive regulation of transcription] evidence: IEA
GeneID:3229 -> Molecular function: GO:0003682 [chromatin binding] evidence: IEA
GeneID:3229 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: NAS
GeneID:3229 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:3229 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA
GeneID:3229 -> Biological process: GO:0001942 [hair follicle development] evidence: IEA
GeneID:3229 -> Biological process: GO:0007275 [multicellular organismal development] evidence: NAS
GeneID:3229 -> Biological process: GO:0009653 [anatomical structure morphogenesis] evidence: TAS
GeneID:3229 -> Biological process: GO:0009952 [anterior/posterior pattern specification] evidence: IEA
GeneID:3229 -> Biological process: GO:0035878 [nail development] evidence: IEA
GeneID:3229 -> Biological process: GO:0043587 [tongue morphogenesis] evidence: IEA
GeneID:3229 -> Cellular component: GO:0005634 [nucleus] evidence: NAS
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